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SENSIMED Triggerfish® Sensor MEDIUM

FDA UDI

Class II (US FDA UDI)

by Sensimed AG

Identity

Trade Name
SENSIMED Triggerfish® Sensor MEDIUM FDA UDI
Generic Name
Ocular volume ambulatory recording system sensor FDA UDI
Device Name
A box of three MEDIUM SENSIMED Triggerfish® Sensors FDA UDI
Model / Reference
M.V.4 FDA UDI
Description
A box of three MEDIUM SENSIMED Triggerfish® Sensors FDA UDI

Identifiers

Catalog Number
BO3M FDA UDI
Primary DI / UDI-DI
07640153470058 FDA UDI
510(k) Number
DEN140017 FDA UDI
FDA Product Code
PLZ FDA UDI
GMDN Term
Ocular volume ambulatory recording system sensor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1925 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Ocular volume ambulatory recording system sensor

SENSIMED Triggerfish® Sensor MEDIUM by Sensimed AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ocular volume ambulatory recording system sensor.

Cleared under the same submission

DEN140017 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sensimed AG

Sources (1)

  • FDA UDI 96f9808e-9ea6-4706-b50a-71378c30f3c1 36 fields · synced Jun 8, 2026